This 31-year-old Nigerian woman had no idea what she was about to go through when she gave birth in February of that year. She can now distinguish her sons’ identical twins with ease. Even though Daniel and David were born only a few minutes apart, they don’t resemble one another at all.
Albinos are both of Stacy and Babajide’s children, who are both black and reside in Lagos. The adorable twins frequently attract attention wherever they go as a result of their noticeably dissimilar appearances. David is stunningly white with pale skin and golden hair, whereas Daniel resembles his 5-year-old big sister Demilade and has dark skin and black curly hair.
After only a year, the twins had nearly 18,000 followers on Instagram thanks to Stacy’s decision to share the odd couple’s activities there.
The twins’ birth on February 26 of last year completely caught everyone off guard.
“We did not know about their differences while I was pregnant, the scan did not show such so it was a huge surprise and the most amazing moment when the first twin (Daniel) came out with black hair and the second twin (David) came out with gold hair. I had them through CS, so the doctors were like: “It seems you are having totally unidentical twins.” Before I knew it, nurses started coming out to look at them,” mum of three, Stacy, explained.
The twins could be clearly distinguished from one another since one was black and the other was white
Stacy shared with us her husband’s heartfelt response to this turn of events.
“Their dad was really overwhelmed and immediately named My Twin 2 (David) ‘Golden,’ so he fondly calls him Mr. Golden. He was all overjoyed seeing his boys. He stood for more than 10 minutes staring at them and said he was just looking at God’s wonderful work and that they are his best gift ever.”
David falls into the highly unusual category of albinism; just 1 in 20,000 infants are born with this condition.
Albinism is a congenital condition that alters appearance due to a lack of melanin, the pigment generated in the skin, hair, and eyes. All racial and ethnic groups are impacted, and the type of pigmentation affects pigmentation to varying degrees. With a birth probability of between 3,000 and 20,000, albinism is a rare condition. Albinos must exercise extreme caution because it may result in a number of skin and vision problems.
David has gorgeous golden hair and an exceptionally pale complexion due to oculocutaneous albinism. Fortunately, Stacy claims that David has no health issues.
Nigeria is one of the nations with the greatest prevalence of albinism in the world with over two million confirmed or suspected cases. However, the statistics show that there is still a lot of prejudice against this community because of the color of its members’ skin. Over 600,000 albino Nigerians experience discrimination and harassment from their peers, family, and communities, which frequently results in difficulties on the job and academic failure.
Stacy did claim that her two sons are both unconditionally and equally adored and that no one has ever said anything unpleasant about them to her.
“There’re always side talks whenever we go out, people often wanna know how and what’s happening and maybe due to their cute and adorable nature, you just wanna come close to say hello.”
The twins’ family has been receiving modeling offers from agencies in the UK due to their odd features. The family is ready to take advantage of any opportunities that may present themselves and has created an Instagram account to share their joy and draw attention to significant issues. Stacy and I decided to create an account for them in order to spread awareness since we believe they have a story to tell.
“They have two different amazing personalities, they are a year+ now, walking and very playful,” said Stacy
“Daniel is more expressive while David is an observer. Both of them are highly inquisitive. Daniel is a foodie while David is quite picky; Daniel is extremely playful while David chooses moments; Daniel always likes to play the bigger brother role; they are both energetic.”
Celine Dion Faces ‘Unimaginable’ Medical Crisis: New Documentary Reveals All!
Celine Dion is giving fans an honest look at her life with stiff person syndrome.
In a new documentary, the famous singer experiences a scary medical crisis during a physical therapy session, and it’s all caught on camera.
In 2022, Dion revealed she had been diagnosed with stiff person syndrome. In the documentary, “I Am: Celine Dion,” she shares that she had been dealing with symptoms of this rare, progressive neurological disorder for 17 years.
“I need my instrument. And my instrument was not working. So we started to elevate the medicine,” Dion, 56, said after struggling to hit certain notes during her 2018 and 2019 tours.
Though she completed her 2018 tour, Dion had to postpone several dates from her 2019 tour due to the “common cold” before the pandemic shut it down.
Her tour resumed in 2022, but she had to keep canceling and rescheduling shows. It wasn’t until she announced her diagnosis that she officially canceled the rest of her appearances.
“I can’t lie anymore,” Dion says in the documentary. “From a sinus infection to an ear infection to whatever. Sometimes I would point my microphone toward the audience, and I would make them sing it. There are moments where I cheated and I tapped on the microphone like it was the microphone’s fault.”
LONDON, ENGLAND – JULY 05: Celine Dion performs live at Barclaycard Presents British Summer Time Hyde Park at Hyde Park on July 05, 2019 in London, England. (Photo by Samir Hussein/Redferns)
In the documentary, there’s a part where Dion shows a very personal moment. She’s lying on a massage table doing exercises for her physical therapy when her foot suddenly starts to cramp. Soon after, her whole body tightens up and she can’t move or talk to the people around her.
The camera keeps recording as another person from her medical team rushes in with a nasal spray called benzodiazepine. They give it to Dion, who’s in so much pain that she’s crying, even though she can’t move. It’s really hard to watch this part of the video.
Once the spasms have subsided – they typically last anywhere from 30 minutes to an hour – Dion is able to sit up and speak.
“Every time something like this happens, it makes me feel so embarrassed,” she says. “I don’t know how to express it, you know, to not have control over yourself.”
Her physical therapist speculates the attack was brought on by being “overstimulated” from an earlier singing session.
“If I can’t get stimulated by what I love, then I’m going to go on stage, and you’re going to put the pulse oximeter on me and turn me on my back?” she wonders.
Dion hopes that one day soon she’ll be able to return to the stage.
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